欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1944/002
药品名称
Propranolol Generis
活性成分
PROPANOL 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Generis Farmacêutica, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Propranolol PUREN 40 mg Filmtabletten
Belgium (BE)
Propranolol AB 40 mg filmomhulde tabletten
Netherlands (NL)
Propranolol HCl Aurobindo 40 mg, filmomhulde tabletten
France (FR)
Spain (ES)
Poland (PL)
Propranolol Aurovitas
许可日期
2019/05/30
最近更新日期
2024/03/08
药物ATC编码
C07AA05 propranolol
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
COMMON FINAL TEXTS
Date of last change:2024/03/08
Final Product Information
|
Labelling
Date of last change:2020/03/09
PAR
|
PAR_proposto
Date of last change:2020/03/09
Final Product Information
|
PIL_clean
Date of last change:2020/03/09
Final Product Information
|
SPC_clean
Date of last change:2020/03/09
市场状态
Positive
©2006-2024
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase